Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2/00—Processes of polymerisation
  • C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation

Definitions

• This invention relates to polymerizable compositions, and more particularly to inhibiting against polymerization compositions which are polymerizable under the influence of heat, light or oxygen and which comprise a polymerizable (more particularly, monomeric) organic compound containing in its molecule the polymerizablegrouping"
• the invention isespecially concerned with liquid polymerizable organic compounds of the kind just stated in which is incorporated a memberhof the class consisting of ascorbic acid, isoascorbic acid, and mixtures of ascorbic and isoascorbicacids in an amount sufficient to inhibit the polymerization of the compound.
• the polymerized compositions which result from practicing this invention contain the decomposition product obtained heat, light or oxygen, the member of. the .class justpdescribed that was incorporated with the polymerizable material.
• Such chemical bodies ashydroquinone, pyrogallol, copper salts and sulfurare used extensively as, inhibitors of polymerization ofmonomeric organic compounds oi. the kind above mentioned, .specific examples of which are. styrene, vinyl.
• esters e. g., vinyl acetate
• esters of acrylic acid e.. g., methyl acry1ate
• .esters of alpha-substituted acrylic acids e. g., methyl methacrylate
• 'Pyrogallol and hydroquinone although removable by distillation, usually are removed by extractionwith dilute, aqueous solutions of alkalies such as sodium hydroxide, followed byv washing with distilled water, and then drying.
• the ideal inhibitor would be a colorless or nearly colorless chemical that would exert an inhibiting eii'ect for a reasonable period of time.
• Another sample was prepared by incorporating 0.1% isoascorbic acid and 0.5% benzoyl peroxide in monomeric methyl metha'crylateg. This sample was polymerized under theisame conditions as the other sample. The hardening'time in both cases was the same, but the isoascorbic acid inhibited methacrylate in polymeric state was much lighter in color than ,the py'rogallol-inhibited material. r (Nata-All percentages herein mentioned are by weight.) p
• sample A was still a liquid and had a yellow cast.
• Example 3 A sample of allyl methacrylate and a sample of allyl methacrylate saturated with isoascorbic acid. were heated to 70 C. in an oven. The noninhibited material became converted to a hard mass in 2 hours. The sample containing the isoascorbic acid was unaffected after 4 heating.
• Example 4 Samples of glycol methacrylate non-inhibited and inhibited by incorporating therewith about 0.08% isoascorbic acid were heated in an oven at about 70 C. The non-inhibited material polymerized to solid state in about or 11 hours while the isoascorbic acid inhibited material was unchanged. 7
• Example 5 A sample of methallyl methacrylate containing about 0.08% isoascorbic acid and a non-inhibited sample of the same material were heated in an oven at about 70 C. At the end of 16 hours the non-inhibited material had polymerized tosolid state while the inhibited material was unchanged.
• Example 6 Samples were prepared as follows A. Commercial copper-acetate stabilized vinyl acetate to which 0.5% benzoyl peroxide was added.
• samples E and F polymerized to a clear, colorless gummy mass. After 24 hours, sample A became gummy A and had a blue color, sample B was partlypolymerized, sample C'was more highly polymerized than sample B, and sample D wasunchanged.
• Example 7 The following samples of methyl methacrylate were prepared and exposed to direct sunlight in Pyrex glass at room temperature, which varied from 55 to 98 F.:-
• sample B After 7, days exposure sample B was almost completely polymerized. After 9 days, sample C started to polymerize, sample G showed appreciable polymerization, while samples A, D, E and F were' unchanged. After 10 days samples C and G were nearly wholly polymerized, and sample B was completely polymerized. After 13 days samples C and G were completely polymerized, samples E and F were partly polymerized, while samples A and D were unchanged. At the end of 20 days samples A and D were completely polymerized to solid state.
• apolymerizable acrylyl grouping derived from acrylic acid
• acrylic and alphalkyl acrylic acids and esters of such acids as, for example, methyl, ethyl, propyl and butyl acrylates, ethyl, propyl and butyl methacrylates, methyl, ethyl, propyl and butyl ethacrylates, and the like.
• Vinyl compounds other than vinyl acetate also may be inhibited as herein described, for example vinyl benzene (styrene), vinyl propionate, vinyl butyrate, etc.
• Ascorbic and isoascorbic acids are readily destroyed in situ by heat and by accelerators of polymerization such as organic peroxides, leaving colorless decomposition products in the polymerized material that need not be removed.
• these acids although not limited thereto, are particularly suitable for use in inhibiting the polymerization of liquid monomeric compounds which in polymeric state should be colorless.
• Ascorbic and isoascorbic acids also maybe used to inhibit the polymerization of other compounds which polymerize under the influence of heat, light or oxygen-containing bodies and which comprise a polyme'rizable organic compound con taming in its molecule the ploymerizable grouping what I claim as new and desire to secure by Letters Patent of the United States is:
• isoascorbic acid and mixtures of ascorbic and isoascorbic acids in an amount suflicient to inhibit the polymerization of the said organic com pound.
• a polymerizable ester of acrylic acid having incorporated therein a member of the class consisting of ascorbic acid, isoascorbic acid, and mixtures of ascorbic and 'isoascorbic acids in an amount suflicient to inhibit the polymerization of the said ester.
• A'polymerizable composition consisting of monomeric methyl methacrylate having incorporated therein isoascorbic acid in an amount sufiicient to inhibit the polymerization of the said methacrylate.
• Apolymerizable composition consisting of a polymerizable ester of an alpha-alkyl acrylic acid having incorporated therein as an inhibitor of polymerization a small amount of a member of the class consisting of ascorbic acid, isoascorbic acid, and mixtures of ascorbic and isoascorbic acids.
• a polymerizable composition consisting of polymerizable vinyl acetate having incorporated therein as an inhibitor of polymerization a small ascorbic acid, isoascorbic acid, and mixtures of ascorbic and isoascorbic acids.
• a composition comprising a. polymerizable organic compound containing in its molecule the polymerizable grouping and, in addition to said compound, ascorbic acid in an amount sufiicient to inhibit the polymerization of the said organic compound.
• a composition comprising a polymerizable organic compound containing in its molecule the polymerizable grouping and, in addition to said compound, isoascorbic acid in an amount suflicient to inhibit the polymerization of the said organic compound.
• a polymerizable organic compolmd containing in its molecule the polymerizable grouping said compound having incorporated therewith as an inhibitor of polymerization from 0.05 to 0.5 per cent by weight thereo! of a member of the class consisting of ascorbic acid, isoascorbic acid and mixtures of ascorbic and isoascorbic acid.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Polymerisation Methods In General (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Priority Applications (3)

Applications Claiming Priority (1)

Publications (1)

Family

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Family Applications (1)

Country Status (3)

Cited By (9)

Families Citing this family (1)

• 1938
  • 1938-10-01 US US232901A patent/US2255483A/en not_active Expired - Lifetime
• 1939
  • 1939-09-30 GB GB26932/39A patent/GB535219A/en not_active Expired
  • 1939-10-02 DE DEL99179D patent/DE706509C/de not_active Expired

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